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  • GEL;TOPICAL - EQ 0.016% BASE
  • INJECTABLE;INJECTION - 10MG/VIAL

Looking for 55-86-7 / Mechlorethamine API manufacturers, exporters & distributors?

Mechlorethamine manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Mechlorethamine API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Mechlorethamine manufacturer or Mechlorethamine supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Mechlorethamine manufacturer or Mechlorethamine supplier.

PharmaCompass also assists you with knowing the Mechlorethamine API Price utilized in the formulation of products. Mechlorethamine API Price is not always fixed or binding as the Mechlorethamine Price is obtained through a variety of data sources. The Mechlorethamine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Mechlorethamine

Synonyms

55-86-7, Chlormethine hydrochloride, Mechlorethamine hcl, Nitrogen mustard hydrochloride, Chlorethamine, 2-chloro-n-(2-chloroethyl)-n-methylethanamine hydrochloride

Cas Number

55-86-7

Unique Ingredient Identifier (UNII)

L0MR697HHI

About Mechlorethamine

A biologic alkylating agent that exerts its cytotoxic effects by forming DNA ADDUCTS and DNA interstrand crosslinks, thereby inhibiting rapidly proliferating cells. The hydrochloride is an antineoplastic agent used to treat HODGKIN DISEASE and LYMPHOMA.

MECHLORETHAMINE HYDROCHLORIDE Manufacturers

A MECHLORETHAMINE HYDROCHLORIDE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MECHLORETHAMINE HYDROCHLORIDE, including repackagers and relabelers. The FDA regulates MECHLORETHAMINE HYDROCHLORIDE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MECHLORETHAMINE HYDROCHLORIDE API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

MECHLORETHAMINE HYDROCHLORIDE Suppliers

A MECHLORETHAMINE HYDROCHLORIDE supplier is an individual or a company that provides MECHLORETHAMINE HYDROCHLORIDE active pharmaceutical ingredient (API) or MECHLORETHAMINE HYDROCHLORIDE finished formulations upon request. The MECHLORETHAMINE HYDROCHLORIDE suppliers may include MECHLORETHAMINE HYDROCHLORIDE API manufacturers, exporters, distributors and traders.

click here to find a list of MECHLORETHAMINE HYDROCHLORIDE suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

MECHLORETHAMINE HYDROCHLORIDE USDMF

A MECHLORETHAMINE HYDROCHLORIDE DMF (Drug Master File) is a document detailing the whole manufacturing process of MECHLORETHAMINE HYDROCHLORIDE active pharmaceutical ingredient (API) in detail. Different forms of MECHLORETHAMINE HYDROCHLORIDE DMFs exist exist since differing nations have different regulations, such as MECHLORETHAMINE HYDROCHLORIDE USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A MECHLORETHAMINE HYDROCHLORIDE DMF submitted to regulatory agencies in the US is known as a USDMF. MECHLORETHAMINE HYDROCHLORIDE USDMF includes data on MECHLORETHAMINE HYDROCHLORIDE's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The MECHLORETHAMINE HYDROCHLORIDE USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of MECHLORETHAMINE HYDROCHLORIDE suppliers with USDMF on PharmaCompass.

MECHLORETHAMINE HYDROCHLORIDE NDC

National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing MECHLORETHAMINE HYDROCHLORIDE as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for MECHLORETHAMINE HYDROCHLORIDE API and other APIs are published in this directory by the FDA.

Unfinished drugs

The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.

Pharmaceutical companies that manufacture MECHLORETHAMINE HYDROCHLORIDE as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.

Compounded drug products

The NDC directory also contains data on finished compounded human drug products that contain MECHLORETHAMINE HYDROCHLORIDE and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a MECHLORETHAMINE HYDROCHLORIDE NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of MECHLORETHAMINE HYDROCHLORIDE suppliers with NDC on PharmaCompass.

MECHLORETHAMINE HYDROCHLORIDE GMP

MECHLORETHAMINE HYDROCHLORIDE Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.

GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).

PharmaCompass offers a list of MECHLORETHAMINE HYDROCHLORIDE GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right MECHLORETHAMINE HYDROCHLORIDE GMP manufacturer or MECHLORETHAMINE HYDROCHLORIDE GMP API supplier for your needs.

MECHLORETHAMINE HYDROCHLORIDE CoA

A MECHLORETHAMINE HYDROCHLORIDE CoA (Certificate of Analysis) is a formal document that attests to MECHLORETHAMINE HYDROCHLORIDE's compliance with MECHLORETHAMINE HYDROCHLORIDE specifications and serves as a tool for batch-level quality control.

MECHLORETHAMINE HYDROCHLORIDE CoA mostly includes findings from lab analyses of a specific batch. For each MECHLORETHAMINE HYDROCHLORIDE CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.

MECHLORETHAMINE HYDROCHLORIDE may be tested according to a variety of international standards, such as European Pharmacopoeia (MECHLORETHAMINE HYDROCHLORIDE EP), MECHLORETHAMINE HYDROCHLORIDE JP (Japanese Pharmacopeia) and the US Pharmacopoeia (MECHLORETHAMINE HYDROCHLORIDE USP).

Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.
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